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U.S. Department of Health and Human Services

Medical Device Recalls
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251 to 260 of 500 Results *
Recall Date to: 09/01/2014
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Product Description
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FDA Recall
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Misys Laboratory, version 5.3 with Reference Laboratory Interface 2 03/13/2003 Sunquest Information Systems
Flexgard, off-the-shelf knee brace, product number 14761106 2 03/19/2003 De Royal Industries
Hybrid Capture II CT-ID Test, Catalog #5135-1050IVT, (labeled for export only). 2 03/19/2003 Digene Corp
Digene''s Hybrid Capture 2 HPV DNA Test, Catalog # 5101-1096 2 03/19/2003 Digene Corp
Digene''s Hybrid Capture 2 HPV DNA Test, Catalog # 5196-1230, labeled for export only. 2 03/19/2003 Digene Corp
Hybrid Capture 2 High-Risk HPV DNA Test, Catalog # 5101-1296 2 03/19/2003 Digene Corp
Fetal Cell Stain Kit No. S0412-00, contents include 3 x 120ml Fetal Cell Fixing Solution (80% Reagen... 2 03/20/2003 Simmler Inc
Baxter 1550 Single Patient System Hemodialysis Machines; Baxter Healthcare Corporation, Deerfield, I... 2 03/20/2003 Baxter Healthcare Corp.
Baxter SPS 550 Single Patient System Hemodialysis Machine; Baxter Healthcare Corporation, Renal Divi... 2 03/20/2003 Baxter Healthcare Corp.
Stretta brand Catheter and Accessory Kit, Part # 175-2575. Model 4301K 2 03/20/2003 Curon Medical Inc

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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